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Dual Anti-glutamate Therapy in Super-refractory Status Epilepticus After Cardiac Arrest
Sponsor: University of Milano Bicocca
Summary
Status epilepticus (SE) is found in 20-30% of patients in coma after cardiac arrest, is often refractory to medical therapy and is considered a negative prognostic factor. Intensity and duration of treatment of refractory and super-refractory post-anoxic SE pose the ethical dilemma between futility of treatments and, conversely, their premature suspension. A recent study by the Epilepsy Center of the San Gerardo Hospital has shown that patients with super-refractory post-anoxic SE and favorable prognostic indicators can achieve a good functional outcome in more than 40% of cases, if treated with intensive and protracted therapy. However, there is profound uncertainty about the best combination of antiseizure medications and anesthetics to use in this condition. A combined anti-glutamatergic therapy with ketamine (anti-NMDA receptor) and perampanel (anti-AMPA receptor), aimed at counteracting the excitotoxicity linked to global cerebral ischemia, could be particularly effective in the treatment of super-refractory SE with post-anoxic etiology. Preliminary results in the first 26 patients treated in the Coordinating Center of the project indicate that this therapy appears safe and highly effective (80% SE resolution, 40% good neurological outcome). The aim of the SUPER-CAT study is to investigate the efficacy and safety of combined therapy with ketamine and perampanel (dual anti-glutamatergic therapy) in patients with post-anoxic super-refractory status epilepticus, compared to other therapies, using a multi-centre, retrospective, cohort study design.
Official title: SUPER-refractory Status Epilepticus After Cardiac Arrest: a Multicenter, Retrospective, Cohort Study of Dual Anti-glutamate Therapy With Ketamine and Perampanel
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
80
Start Date
2022-01-15
Completion Date
2025-09-30
Last Updated
2025-07-29
Healthy Volunteers
No
Conditions
Interventions
Ketamine
"Dual anti-glutamatergic therapy" (DUAL) intervention group: patients who received ketamine as a continuous i.v. for 3 days (induction dose 1.5-3 mg/kg, followed by maintenance dose 2-10 mg/kg/h; dose adjustment according to EEG target of "ketamine pattern") + oral perampanel via nasogastric tube for 5 days (12 mg if weight \> 60 kg; 9 mg if weight 50-60 kg; 6 mg if weight \< 50 kg), followed by gradual reduction according to clinical evolution.
Any anti-epileptic and anesthetic therapy, excluding Ketamine and Perampanel
Any antiseizure and anesthetic therapy according to usual clinical practice, excluding the two anti-glutamate drugs Ketamine and Perampanel
Locations (10)
ASST Spedali Civili Brescia
Brescia, BS, Italy
Ospedale Centrale di Bolzano
Bolzano, BZ, Italy
Ospedale G. Brotzu
Cagliari, CA, Italy
Ospedale M. Bufalini
Cesena, FC, Italy
AOU Careggi
Florence, FI, Italy
Fondazione IRCCS San Gerardo dei Tintori Monza
Monza, MB, Italy
Azienda Ospedaliero-Universitaria di Modena
Modena, MO, Italy
Azienda Ospedaliero-Universitaria di Parma
Parma, PR, Italy
Ospedale Santa Chiara Trento
Trento, TN, Italy
Azienda Ospedaliero-Universitaria Integrata di Verona
Verona, VR, Italy